A Clinical Trial of TQ05105 Tablets Combined With TQB3909 Tablets in the Treatment of Myelofibrosis (MF)

Phase 1

Recruiting

• Conditions: Myelofibrosis
• Interventions: Drug: TQB3909 tablets; Drug: TQ05105 tablets

• Registration Number: NCT06245941
• Lead Sponsor: Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

Brief Summary

This is an open, single-arm, multi-center clinical study designed to evaluate the efficacy and safety of TQ05105 tablets combined with TQB3909 tablets in patients with moderate- and high-risk Myelofibrosis.

Detailed Description

Not available

Study Timeline

• Status Verified: 2024-01
• Study First Submitted: 2024-01-30
• Study First Submitted QC: 2024-01-30
• Study First Posted: 2024-02-07
• Study Start: 2024-05-13
• Last Update Submitted: 2024-07-24
• Last Update Posted: 2024-07-25
• Primary Completion: 2026-06
• Study Completion: 2027-05

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 93

Inclusion Criteria

• Voluntarily participate in the study and signed informed consent with good compliance;
• Age: 18 or above (when signing the informed consent form); Eastern Cooperative Oncology Group (ECOG) performance status (PS) score of 0 to 2; Life expectancy ≥ 24 weeks;
• Patients diagnosed with Primary myelofibrosis (PMF), post polycythemia vera myelofibrosis (post-PV-MF), or post essential thrombocythemia myelofibrosis (post-ET-MF);
• Those with moderate or high risk myelofibrosis evaluated according to Dynamic International Prognostic Scoring System (DIPSS) prognostic grading criteria, or those with high risk myelofibrosis according to National Comprehensive Cancer Network (NCCN) guidelines prognostic grading criteria;
• Patients with poor efficacy of JAK inhibitors (for monotherapy of TQB3909, phase Ib and phase II cohort 2);
• Patients who had not received JAK inhibitor treatment (for phase II cohort 1)
• Spleen enlargement;
• Peripheral blood primary cells and bone marrow primary cells are ≤10%;
• No growth factor, colony stimulating factor, thrombopoietin or platelet transfusion was received within 2 weeks before the examination, and the blood routine indexes met the requirements within 7 days before the first administration
• The Main organ function is normal;
• Men and women of childbearing age should agree to use contraceptive measures during the study period and within 6 months after the end of the study.

Exclusion Criteria

• Patients who have previously received allogeneic stem cell transplantation, or received autologous stem cell transplantation within 3 months before the first administration, or recently planned stem cell transplantation;
• Patients who have previously received BCL-2 inhibitor combined with JAK inhibitor therapy;
• Patients who have previously undergone splenectomy, or received splenic radiotherapy within 6 months before the first administration;
• Other malignancies within 3 years prior to first administration or currently present.
• Patients with multiple factors affecting oral or absorption of drugs;
• Major surgical treatment or significant traumatic injury within 4 weeks prior to first administration;
• Presence of congenital bleeding disorder and congenital coagulopathy;
• Patients who had arterial/venous thrombosis events within 6 months before the first administration.
• Have a history of mental drug abuse, or have a mental disorder.
• Active or uncontrolled severe infection;
• Active hepatitis B virus (HBV) infection, or hepatitis C virus (HCV) infection , or active Corona Virus Disease 2019 (COVID-19) infection;
• Patients with grade III or above congestive heart failure, unstable angina pectoris or myocardial infarction, or arrhythmia requiring treatment, or QT interval prolongation within 6 months before the first administration;
• Unsatisfactory blood pressure control despite standard therapy;
• Patients with renal failure requiring hemodialysis or peritoneal dialysis;
• Patients newly diagnosed with pulmonary interstitial fibrosis or drug-related interstitial lung disease within 3 months before the first administration;
• Patients with a history of immunodeficiency disease or organ transplantation;
• Patients with epilepsy requiring treatment;
• Patients with uncontrolled pleural effusion, pericardial effusion or ascites;
• There is a history of attenuated live vaccine inoculation within 4 weeks before the first administration, or attenuated live vaccine inoculation was planned during the study period.
• People with known hypersensitivity to the study drug and excipients;
• Patients diagnosed as active autoimmune diseases within 2 years before the first administration;
• Those who participated in and used other anti-tumor clinical trial drugs within 4 weeks before the first administration
• Any MF treatment drugs, any immunomodulators, or any immunosuppressants were used within 2 weeks prior to the first dose
• According to the judgment of the investigators, some situations seriously endanger the safety of the subjects or affect the subjects to complete the study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
TQB3909 Tablets	TQB3909 tablets	TQB3909 Tablets, orally administered. 28 days as a treatment cycle.
TQ05105 Tablets combined with TQB3909 Tablets	TQ05105 tablets	TQ05105 Tablets combined with TQB3909 Tablets, orally administered. 28 days as a treatment cycle.
TQ05105 Tablets combined with TQB3909 Tablets	TQB3909 tablets	TQ05105 Tablets combined with TQB3909 Tablets, orally administered. 28 days as a treatment cycle.

Primary Outcome Measures

Name	Time	Method
Maximal tolerance dose (MTD)	Up to 2 years.	If dose limiting toxicity (DLT) occurs in 2 or more subjects in a given dose group, the dose level in the previous dose group is considered as MTD.
35% reduction in spleen volume (SVR35) at week 24	Up to 24 weeks	The proportion of subjects with a ≥35% reduction in spleen volume from baseline at the end of treatment at week 24
Recommended phase II dose (RP2D)	Up to 2 years	The RP2D is defined as the lower dose level to MTD based on the safety profile

Secondary Outcome Measures

Name	Time	Method
Percentage change in spleen volume from baseline	Up to 60 weeks	Percentage change in spleen volume of subjects from baseline after treatment.
Onset time of splenic response	Up to 120 weeks	The time interval from the first administration to the date when the spleen volume was reduced by ≥ 35 % from baseline
SVR35 at week 60	Up to 60 weeks	The proportion of subjects with a ≥35% reduction in spleen volume compared to baseline after treatment at week 60.
Myeloproliferative neoplasm - Symptom Assessment Form - Total Symptom Score (MPN-SAF-TSS)	Up to 60 weeks	The proportion of subjects whose total symptom score of MPN-SAF TSS decreased by more than 50% from baseline. MPN-SAF-TSS is a tool for evaluating the disease burden of patients with myeloproliferative neoplasms. Each symptom is scored according to the severity, from asymptomatic (0 points) to the most serious (10 points), a total of 10 levels, the sum of 10 symptom scores is MPN-SAF-TSS score. The higher the score, the more severe the symptoms are.
Duration of maintenance of at least 35% Reduction in Spleen Volume (DoMSR)	Up to 120 weeks	The time between the date when the spleen volume reduction ≥ 35% from baseline occurs for the first time and the date when the spleen volume reduction is \< 35% from baseline.
Progression-free survival (PFS)	Up to 120 weeks	The time interval from the first dose to the date of the occurrence of any of the following events, whichever occurs first:(1) Spleen volume increased by ≥25% compared with the screening period ; (2) Death caused by any cause.
Leukemia free survival (LFS)	Up to 120 weeks	The time interval from the date of the first dose to the date of any of the following events, whichever occurs first: (1) the date of the first bone marrow smear showing the original cell ≥20% ;(2) The first peripheral blood smear showed that the original cells ≥ 20% and the absolute value of the original cells ≥1×10\^9/L and lasted for at least 2 weeks; (3) Death caused by any reason.
Overall Survival (OS)	Up to 120 weeks	The time from the first time the subject received treatment to death due to any cause
Optimum effective rate	Up to 120 weeks	The proportion of subjects with at least once spleen volume reduction ≥ 35% from baseline
Severity of adverse events (AEs)	Baseline up to 120 weeks	Severity of all adverse medical events that occur after the subject receives the investigational drug, evaluated according to the Common Terminology Criteria for Adverse Events Version 5.0 (CTCAE v5.0)
MPN-SAF-TSS decrease	Up to 60 weeks	The time and duration when the MPN-SAF-TSS decreased by ≥50% compared to baseline for the first time.
Incidence of adverse events (AEs)	Baseline up to 120 weeks	Incidence rate of all adverse medical events that occur after the subject receives the investigational drug, evaluated according to the Common Terminology Criteria for Adverse Events Version 5.0 (CTCAE v5.0)

Trial Locations

Locations (5)

Hennan Cancer Hospital; 🇨🇳 Zhengzhou, Henan, China

Xijing Hospital of the Fourth Military Medical University; 🇨🇳 Xian, Shaanxi, China

The Second People's Hospital of Hefei; 🇨🇳 Hefei, Anhui, China

The First Affiliated Hospital Zhejiang University School Of Medicine; 🇨🇳 Hangzhou, Zhejiang, China

People's Hospital of Tianjin; 🇨🇳 Tianjin, Tianjin, China